Policy & Regulations

This channel includes news coverage of healthcare policy and regulations set by Congress, the states, Centers for Disease Control and Prevention (CDC), the Department of Health and Human Services (HHS), U.S. Food and Drug Administration (FDA), and medical associations and societies. 

Colorized scanning electron micrograph of monkeypox virus (orange) on the surface of infected VERO E6 cells (green). Credit: NIAID

Monkeypox declared public health emergency

HHS Secretary Xavier Becerra made the announcement Aug. 4 in recognition of the continued rapid transmission of monkeypox in the U.S. and globally.

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Justice Department sues Idaho over abortion ban

The move comes after the Biden administration clarified that abortions are still accessible as emergency care in all states, as per federal law.

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UnitedHealth’s battle over $13B merger begins

The trial to decide if UnitedHealth Group will be allowed to pursue its $13 billion acquisition with Change Healthcare is underway.

Cardiologist-backed bill focused on the heart health of South Asian Americans gains momentum

After successfully making it through the House, the new legislation is now headed to the Senate. 

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Cardiologists, radiologists join American Medical Association to speak out against ACA lawsuit

Yet another lawsuit is taking aim at the Affordable Care Act, and 61 U.S. medical organizations have joined forces to speak out.

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Federal agencies reinforce contraceptive coverage guidance

“Under the ACA, you have the right to free birth control — no matter what state you live in," HHS Secretary Xavier Becerra said.

 

contraceptive pills

Cleveland Clinic offering Saturday appointments dedicated to contraceptive care

“Reproductive healthcare decisions are best made between a patient and their healthcare provider. It is critical that women and men have immediate access to contraception," says Tristi Muir, MD, chair of the Obstetrics, Gynecology & Women’s Health Institute at Cleveland Clinic.

House votes to extend telehealth benefits

The bill, Advancing Telehealth Beyond COVID–19 Act of 2022, extends telehealth flexibilities under Medicare that were initially authorized during the public health emergency relating to COVID-19.

Around the web

Cardiovascular devices are more likely to be in a Class I recall than any other device type. The FDA's approval process appears to be at least partially responsible, though the agency is working to make some serious changes. We spoke to a researcher who has been tracking these data for years to learn more. 

Updated compensation data includes good news for multiple subspecialties. The new report also examines private equity's impact on employment models and how much male cardiologists earn compared to females.

When drugs are on the FDA’s shortage list, outsourcing facilities can produce their own compounded versions. When the FDA removed tirzepatide from that list with no warning, it created a considerable amount of chaos both behind the scenes and in pharmacies all over the country. 

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